Pages that link to "Q37467854"

The following pages link to Colorectal cancer risk variants on 11q23 and 15q13 are associated with unexplained adenomatous polyposis (Q37467854):

Displayed 16 items.

• Unsupervised Analysis of Array Comparative Genomic Hybridization Data from Early-Onset Colorectal Cancer Reveals Equivalence with Molecular Classification and Phenotypes. (Q31149689) ‎ (← links)
• Common colorectal cancer risk alleles contribute to the multiple colorectal adenoma phenotype, but do not influence colonic polyposis in FAP. (Q34075491) ‎ (← links)
• Germline variants in POLE are associated with early onset mismatch repair deficient colorectal cancer (Q35154300) ‎ (← links)
• Clinical relevance of 8q23, 15q13 and 18q21 SNP genotyping to evaluate colorectal cancer risk (Q36695815) ‎ (← links)
• Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis (Q37153032) ‎ (← links)
• Risk of eighteen genome-wide association study-identified genetic variants for colorectal cancer and colorectal adenoma in Han Chinese (Q37718414) ‎ (← links)
• Copy number variants associated with 18p11.32, DCC and the promoter 1B region of APC in colorectal polyposis patients (Q39973575) ‎ (← links)
• Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers. (Q39994844) ‎ (← links)
• Germline deletions in the tumour suppressor gene FOCAD are associated with polyposis and colorectal cancer development. (Q41356138) ‎ (← links)
• Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia (Q41532605) ‎ (← links)
• Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis (Q44577314) ‎ (← links)
• Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas (Q48404100) ‎ (← links)
• Common genetic variants (rs4779584 and rs10318) at 15q13.3 contributes to colorectal adenoma and colorectal cancer susceptibility: evidence based on 22 studies. (Q53160558) ‎ (← links)
• Clinical management of hereditary colorectal cancer syndromes (Q62978110) ‎ (← links)
• Rare loss of function variants in candidate genes and risk of colorectal cancer (Q64460727) ‎ (← links)
• Declining detection rates for APC and biallelic MUTYH variants in polyposis patients, implications for DNA testing policy (Q90135262) ‎ (← links)